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Chemical Structure| 15047-76-4 Chemical Structure| 15047-76-4

Structure of 15047-76-4

Chemical Structure| 15047-76-4

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Product Details of [ 15047-76-4 ]

CAS No. :15047-76-4
Formula : C12H12O2
M.W : 188.22
SMILES Code : COC1=CC=C(CC2=CC=CO2)C=C1

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Application In Synthesis of [ 15047-76-4 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 15047-76-4 ]

[ 15047-76-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-00-9 ]
  • [ 104-21-2 ]
  • [ 15047-76-4 ]
YieldReaction ConditionsOperation in experiment
48% With proton-exchanged montmorillonite; at 20℃; General procedure: To a mixture of 12 (66 mg, 0.366 mmol) and arenes or heteroarenes(1 mL) was added H-mont (260 mg). The reaction mixturewas stirred at room temperature until the TLC indicated the consumptionof the starting material. The mixture was filtered toremove H-mont, and the filtrate was evaporated under reducedpressure. The residue was purified by flash chromatography (petroleumether/ethyl acetate 200:1 to 10:1) to give the product.Following the procedure, 14ceg were prepared.
72%Chromat. With trifluorormethanesulfonic acid; In dichloromethane; at 20℃; for 0.166667h; General procedure: 430 muL of anisyl acetate (2.5 mmol, 1 equiv) and 2.2 mL of anisole (12.25 mmol, 5 equiv) were placed into a 10 mL round-bottom flask equipped with a magnetic stir-bar. Then 11 muL 5% of pure triflic acid (0.125 mmol) was added and the solution was stirred for 20 min. The crude was analyzed by 1H NMR and GC-MS. Purification by column chromatography gave 484 mg (85% yield) of bis(4-methoxyphenyl)methane, which was identical to an authentic sample.
 

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